Rocuronium
- Product NDC
- 71872-7349
- 11-digit product format
- 718727349
- Labeler code
- 71872
- Product ID
- 71872-7349_41efca22-7a41-91b1-e063-6294a90a8018
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Rocuronium
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Medical Purchasing Solutions, LLC.
- Application
- ANDA210437
- Marketing category
- ANDA
- Marketing start
- 2020-07-20
- Substance
- ROCURONIUM BROMIDE
- Active strength
- 100 mg/10mL
- Pharmacologic classes
- Neuromuscular Nondepolarizing Blockade [PE], Nondepolarizing Neuromuscular Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Rocuronium
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ROCURONIUM BROMIDE | 100 mg/10mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | I65MW4OFHZ |
| Rxcui | 1234995 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 71872-7349-1 | Rocuronium | 1 in 1 BAG | INJECTION, SOLUTION | 1 | | 1 |
| 71872-7349-1 | Rocuronium | 10 mL in 1 VIAL | INJECTION, SOLUTION | 10 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71872-7349-1 | 71872734901 | 1 VIAL in 1 BAG (71872-7349-1) / 10 mL in 1 VIAL | 1 vial | 2025-04-21 | No | No | Historical |